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Origins and Mechanisms of miRNAs and siRNAs

Cell, 2009-02, Vol.136 (4), p.642-655

2009

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CRISPR Interference Limits Horizontal Gene Transfer in Staphylococci by Targeting DNA

Science (American Association for the Advancement of Science), 2008-12, Vol.322 (5909), p.1843-1845

2008

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Naturally Occurring Off-Switches for CRISPR-Cas9

Cell, 2016-12, Vol.167 (7), p.1829-1838.e9

2016

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Processing-Independent CRISPR RNAs Limit Natural Transformation in Neisseria meningitidis

Molecular cell, 2013-05, Vol.50 (4), p.488-503

2013

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Efficient genome engineering in human pluripotent stem cells using Cas9 from Neisseria meningitidis

Proceedings of the National Academy of Sciences - PNAS, 2013-09, Vol.110 (39), p.15644-15649

2013

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Improved prime editors enable pathogenic allele correction and cancer modelling in adult mice

Nature communications, 2021-04, Vol.12 (1), p.2121-13, Article 2121

2021

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Assembly and function of RNA silencing complexes

Nature reviews. Molecular cell biology, 2005-02, Vol.6 (2), p.127-138

Sontheimer, Erik J

2005

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Adenovirus-Mediated Somatic Genome Editing of Pten by CRISPR/Cas9 in Mouse Liver in Spite of Cas9-Specific Immune Responses

Human gene therapy, 2015-07, Vol.26 (7), p.432-442

2015

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All-in-one adeno-associated virus delivery and genome editing by Neisseria meningitidis Cas9 in vivo

Genome Biology, 2018-09, Vol.19 (1), p.137-137, Article 137

2018

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Tissue-restricted genome editing in vivo specified by microRNA-repressible anti-CRISPR proteins

RNA (Cambridge), 2019-11, Vol.25 (11), p.1421-1431

2019

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A Cas9 with PAM recognition for adenine dinucleotides

Nature communications, 2020-05, Vol.11 (1), p.2474-2474, Article 2474

2020

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DNase H Activity of Neisseria meningitidis Cas9

Molecular cell, 2015-10, Vol.60 (2), p.242-255

2015

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Template-jumping prime editing enables large insertion and exon rewriting in vivo

Nature communications, 2023-06, Vol.14 (1), p.3369-3369, Article 3369

2023

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CRISPR/Cas9-mediated genome editing induces exon skipping by alternative splicing or exon deletion

Genome Biology, 2017-06, Vol.18 (1), p.108-8, Article 108

2017

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Heavily and fully modified RNAs guide efficient SpyCas9-mediated genome editing

Nature communications, 2018-07, Vol.9 (1), p.2641-9, Article 2641

2018

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Self-inactivating, all-in-one AAV vectors for precision Cas9 genome editing via homology-directed repair in vivo

Nature communications, 2021-11, Vol.12 (1), p.6267-6267, Article 6267

2021

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Crispr: Biology and Applications

1st edition, 2022

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CRISPR-enhanced human adipocyte browning as cell therapy for metabolic disease

Nature communications, 2021-11, Vol.12 (1), p.6931-6931, Article 6931

2021

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NmeCas9 is an intrinsically high-fidelity genome-editing platform

Genome Biology, 2018-12, Vol.19 (1), p.214-214, Article 214

2018

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CRISPR/Cas9-mediated excision of ALS/FTD-causing hexanucleotide repeat expansion in C9ORF72 rescues major disease mechanisms in vivo and in vitro

Nature communications, 2022-10, Vol.13 (1), p.6286-17, Article 6286

2022

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Domain-inlaid Nme2Cas9 adenine base editors with improved activity and targeting scope

Nature communications, 2024-02, Vol.15 (1), p.1458-1458, Article 1458

2024

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Potent Cas9 Inhibition in Bacterial and Human Cells by AcrIIC4 and AcrIIC5 Anti-CRISPR Proteins

mBio, 2018-12, Vol.9 (6)

2018

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Intratracheally administered LNA gapmer antisense oligonucleotides induce robust gene silencing in mouse lung fibroblasts

Nucleic acids research, 2022-08, Vol.50 (15), p.8418-8430

2022

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Silence from within: Endogenous siRNAs and miRNAs

Cell, 2005-07, Vol.122 (1), p.9-12

2005

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Inhibition of CRISPR-Cas9 ribonucleoprotein complex assembly by anti-CRISPR AcrIIC2

Nature communications, 2019-06, Vol.10 (1), p.2806-11, Article 2806

2019

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Origins and Mechanisms of miRNAs and siRNAs

CRISPR Interference Limits Horizontal Gene Transfer in Staphylococci by Targeting DNA

Naturally Occurring Off-Switches for CRISPR-Cas9

Processing-Independent CRISPR RNAs Limit Natural Transformation in Neisseria meningitidis

Efficient genome engineering in human pluripotent stem cells using Cas9 from Neisseria meningitidis

Improved prime editors enable pathogenic allele correction and cancer modelling in adult mice

Assembly and function of RNA silencing complexes

Adenovirus-Mediated Somatic Genome Editing of Pten by CRISPR/Cas9 in Mouse Liver in Spite of Cas9-Specific Immune Responses

All-in-one adeno-associated virus delivery and genome editing by Neisseria meningitidis Cas9 in vivo

Tissue-restricted genome editing in vivo specified by microRNA-repressible anti-CRISPR proteins

A Cas9 with PAM recognition for adenine dinucleotides

DNase H Activity of Neisseria meningitidis Cas9

Template-jumping prime editing enables large insertion and exon rewriting in vivo

CRISPR/Cas9-mediated genome editing induces exon skipping by alternative splicing or exon deletion

Heavily and fully modified RNAs guide efficient SpyCas9-mediated genome editing

Self-inactivating, all-in-one AAV vectors for precision Cas9 genome editing via homology-directed repair in vivo

Crispr: Biology and Applications

CRISPR-enhanced human adipocyte browning as cell therapy for metabolic disease

NmeCas9 is an intrinsically high-fidelity genome-editing platform

CRISPR/Cas9-mediated excision of ALS/FTD-causing hexanucleotide repeat expansion in C9ORF72 rescues major disease mechanisms in vivo and in vitro

Domain-inlaid Nme2Cas9 adenine base editors with improved activity and targeting scope

Potent Cas9 Inhibition in Bacterial and Human Cells by AcrIIC4 and AcrIIC5 Anti-CRISPR Proteins

Intratracheally administered LNA gapmer antisense oligonucleotides induce robust gene silencing in mouse lung fibroblasts

Silence from within: Endogenous siRNAs and miRNAs

Inhibition of CRISPR-Cas9 ribonucleoprotein complex assembly by anti-CRISPR AcrIIC2

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